Incidental Mutation 'IGL02136:Or11g2'
| ID |
281312 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Or11g2
|
| Ensembl Gene |
ENSMUSG00000053815 |
| Gene Name |
olfactory receptor family 11 subfamily G member 2 |
| Synonyms |
MOR106-13P, GA_x6K02T2PMLR-6326342-6327313, Olfr744 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.094)
|
| Stock # |
IGL02136
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
14 |
| Chromosomal Location |
50855681-50856652 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 50855708 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 10
(S10P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148954
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000066457]
[ENSMUST00000213668]
[ENSMUST00000216690]
|
| AlphaFold |
Q7TRM0 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000066457
AA Change: S10P
PolyPhen 2
Score 0.857 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000066496
Gene: ENSMUSG00000053815
AA Change: S10P
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_4
|
35 |
312 |
2.9e-48 |
PFAM |
|
Pfam:7tm_1
|
45 |
294 |
1.4e-19 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000213668
AA Change: S10P
PolyPhen 2
Score 0.857 (Sensitivity: 0.83; Specificity: 0.93)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000216690
AA Change: S10P
PolyPhen 2
Score 0.857 (Sensitivity: 0.83; Specificity: 0.93)
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca12 |
G |
T |
1: 71,286,301 (GRCm39) |
T2511K |
probably damaging |
Het |
| Acta2 |
T |
A |
19: 34,229,230 (GRCm39) |
D53V |
probably damaging |
Het |
| Banf1 |
G |
A |
19: 5,415,098 (GRCm39) |
A71V |
probably benign |
Het |
| Cacng5 |
A |
T |
11: 107,772,557 (GRCm39) |
I97N |
probably benign |
Het |
| Clec14a |
T |
A |
12: 58,315,415 (GRCm39) |
E69V |
probably damaging |
Het |
| Cracr2a |
T |
C |
6: 127,606,893 (GRCm39) |
|
probably benign |
Het |
| Dysf |
A |
G |
6: 84,085,149 (GRCm39) |
R845G |
probably benign |
Het |
| Dzip3 |
T |
C |
16: 48,747,945 (GRCm39) |
N949S |
possibly damaging |
Het |
| Eprs1 |
T |
G |
1: 185,117,180 (GRCm39) |
W408G |
probably damaging |
Het |
| Fgf14 |
G |
A |
14: 124,217,784 (GRCm39) |
P240S |
possibly damaging |
Het |
| Fpgt |
G |
T |
3: 154,798,989 (GRCm39) |
A2E |
probably benign |
Het |
| Galntl5 |
T |
A |
5: 25,425,060 (GRCm39) |
S392R |
probably benign |
Het |
| Gatd1 |
A |
G |
7: 140,988,873 (GRCm39) |
*221Q |
probably null |
Het |
| Gcsam |
T |
A |
16: 45,430,896 (GRCm39) |
M1K |
probably null |
Het |
| Ksr2 |
A |
G |
5: 117,754,959 (GRCm39) |
N351S |
possibly damaging |
Het |
| Map1a |
T |
C |
2: 121,130,693 (GRCm39) |
V503A |
probably damaging |
Het |
| Myl12a |
T |
A |
17: 71,303,851 (GRCm39) |
K9* |
probably null |
Het |
| Ncapg2 |
A |
T |
12: 116,424,203 (GRCm39) |
M1129L |
probably benign |
Het |
| Or8k41 |
T |
C |
2: 86,313,809 (GRCm39) |
I92M |
probably damaging |
Het |
| Otof |
T |
C |
5: 30,531,336 (GRCm39) |
K1691E |
possibly damaging |
Het |
| Pdk4 |
A |
T |
6: 5,486,715 (GRCm39) |
M353K |
probably damaging |
Het |
| Pkhd1 |
A |
T |
1: 20,345,839 (GRCm39) |
W2730R |
probably damaging |
Het |
| Pkn2 |
T |
A |
3: 142,559,351 (GRCm39) |
K58I |
probably damaging |
Het |
| Plk5 |
T |
C |
10: 80,199,001 (GRCm39) |
|
probably null |
Het |
| Prkcq |
T |
C |
2: 11,265,479 (GRCm39) |
F399L |
probably benign |
Het |
| Ptprz1 |
G |
A |
6: 22,972,821 (GRCm39) |
V244M |
probably damaging |
Het |
| Rpusd2 |
T |
C |
2: 118,868,659 (GRCm39) |
F361L |
probably damaging |
Het |
| Rttn |
T |
A |
18: 89,064,252 (GRCm39) |
L1168I |
possibly damaging |
Het |
| S100a9 |
T |
C |
3: 90,600,075 (GRCm39) |
H107R |
probably benign |
Het |
| Serpinb3a |
T |
A |
1: 106,974,015 (GRCm39) |
M299L |
probably benign |
Het |
| Slfn8 |
G |
A |
11: 82,894,291 (GRCm39) |
Q783* |
probably null |
Het |
| Smc3 |
T |
C |
19: 53,624,147 (GRCm39) |
I721T |
probably benign |
Het |
| Top2b |
C |
A |
14: 16,407,103 (GRCm38) |
|
probably benign |
Het |
| Uvssa |
T |
A |
5: 33,549,192 (GRCm39) |
W351R |
probably damaging |
Het |
| Vmn2r107 |
G |
T |
17: 20,595,168 (GRCm39) |
V574L |
probably benign |
Het |
| Wdr3 |
G |
A |
3: 100,046,041 (GRCm39) |
R931* |
probably null |
Het |
|
| Other mutations in Or11g2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01373:Or11g2
|
APN |
14 |
50,856,069 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02165:Or11g2
|
APN |
14 |
50,856,468 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02207:Or11g2
|
APN |
14 |
50,856,015 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02556:Or11g2
|
APN |
14 |
50,856,185 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02710:Or11g2
|
APN |
14 |
50,856,255 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0127:Or11g2
|
UTSW |
14 |
50,855,789 (GRCm39) |
missense |
probably benign |
|
|
R0389:Or11g2
|
UTSW |
14 |
50,856,036 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0603:Or11g2
|
UTSW |
14 |
50,855,967 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0927:Or11g2
|
UTSW |
14 |
50,856,044 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R1477:Or11g2
|
UTSW |
14 |
50,856,170 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1705:Or11g2
|
UTSW |
14 |
50,856,579 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1800:Or11g2
|
UTSW |
14 |
50,856,143 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1898:Or11g2
|
UTSW |
14 |
50,856,231 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2244:Or11g2
|
UTSW |
14 |
50,856,114 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4731:Or11g2
|
UTSW |
14 |
50,856,026 (GRCm39) |
missense |
probably benign |
0.11 |
|
R4732:Or11g2
|
UTSW |
14 |
50,856,026 (GRCm39) |
missense |
probably benign |
0.11 |
|
R4733:Or11g2
|
UTSW |
14 |
50,856,026 (GRCm39) |
missense |
probably benign |
0.11 |
|
R4801:Or11g2
|
UTSW |
14 |
50,856,479 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4802:Or11g2
|
UTSW |
14 |
50,856,479 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5068:Or11g2
|
UTSW |
14 |
50,856,197 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5069:Or11g2
|
UTSW |
14 |
50,856,197 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5070:Or11g2
|
UTSW |
14 |
50,856,197 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5070:Or11g2
|
UTSW |
14 |
50,855,931 (GRCm39) |
missense |
probably benign |
0.11 |
|
R5195:Or11g2
|
UTSW |
14 |
50,856,243 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6058:Or11g2
|
UTSW |
14 |
50,856,158 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8246:Or11g2
|
UTSW |
14 |
50,855,841 (GRCm39) |
missense |
probably benign |
|
|
R8275:Or11g2
|
UTSW |
14 |
50,855,868 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9292:Or11g2
|
UTSW |
14 |
50,856,513 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
| Posted On |
2015-04-16 |
Incidental Mutation